نتایج جستجو برای: gene carrier

تعداد نتایج: 1203376  

Introduction: Hemophilia B is an X-linked recessive genetic disease caused by mutations in the coagulation Factor IX gene. Mutations in the Factor IX gene result in dysfunction or deficiency of coagulation factor of IX. Direct mutation analysis involves the ideal method for molecular diagnosis of the disease. However, due to the high number of identified mutations in the gen, the lack of a comm...

Journal: :The Journal of Cell Biology 1981
K M Huttner J A Barbosa G A Scangos D D Pratcheva F H Ruddle

DNA-mediated gene transfer is a procedure which uses purified DNA to introduce new genetic elements into cells in culture. The standard DNA-mediated gene transfer procedure involves the use of whole cell DNA as carrier DNA for the transfer. We have modified the standard DNA-mediated gene transfer procedure to transfer the Herpes simplex virus type 1 thymidine kinase gene (TK) into TK- murine re...

Journal: :journal of cell and molecular research 0
elham abedheydari mohammad khalaj-kondori mohammad-ali hosseinpour-faizi morteza kosari-nasab

gene delivery might be affected by several tribulations based on carrier/vector applied. bacteriophages lambda and m13 have different genome conformations; linear double-stranded and circular single-stranded respectively. therefore, it might be expected that these two common classes of gene delivery vehicles will have different capacity for gene delivery and expression in eukaryote cells. to ad...

Journal: :journal of arthropod-borne diseases 0
maría guadalupe montes-cortés parasitology and parasitological diseases, veterinary faculty, universidad de extremadura, cáceres, spain josé luis fernández-garcía genetics and animal breeding, veterinary faculty, universidad de extremadura, cáceres, spain miguel ángel habela martínez-estéllez parasitology and parasitological diseases, veterinary faculty, universidad de extremadura, cáceres, spain

background: equine piroplasmosis is caused by two haemoprotozoan parasites: babesia caballi and theileria equi . negative economic impact on international trade has been associated to endemic sites. this is the reason why carrier detection requires reliable diagnostic methods. various diagnostic modalities can be used alone or in combination including pcr. however, genetic variation of commonly...

Journal: :iranian journal of basic medical sciences 0
tahereh moradi division of genetics, department of biology, faculty of science, university of isfahan, isfahan, iran reihaneh vallian molecular genetics department, isfahan medical genetics center, isfahan, iran zahra fazeli department of genetics, faculty of medicine, shahid beheshti university of medical sciences, tehran, iran asieh haghighatnia molecular genetics department, isfahan medical genetics center, isfahan, iran sadeq vallian division of genetics, department of biology, faculty of science, university of isfahan, isfahan, iran molecular genetics department, isfahan medical genetics center, isfahan, iran

objective(s): iran is considered as one of the high-prevalence areas for β-thalassemia with a rate of about 10% carrier frequency. molecular diagnosis of the disease is performed both by direct sequencing and indirectly by the use of polymorphic markers present in the beta globin gene cluster. however, to date there is no reliable information on the application of the markers in the iranian pop...

اشراقی, پریسا, هدایتی, مهدی, دانشپور, مریم‌السادات, عزیزی, فریدون, میرمیران, پروین,

    Background & Aim: There are many articles on the association between β3-adrenoreceptor gene polymorphisms and obesity. The aim of this study was to investigate the association between β3-adrenoreceptor gene polymorphism and serum concentration of Leptin with body mass index(BMI). Materials and Methods: The study was cross-sectional. Participants of Tehran Lipid and Glucose Study were divide...

Journal: :Haematologica 2007
Adoración Venceslá María Jesús Barceló Manel Baena Manuel Quintana Montserrat Baiget Eduardo F Tizzano

Approximately 3% of hemophilia B patients have major deletions in the F9 gene, half of which are complete. Marker and quantitative PCR analyses were employed for carrier diagnosis in a family of a mentally retarded hemophilia B patient with a total deletion of the F9 gene and neighbor genes. Both methodologies allowed the confirmation of carrier or non-carrier status.

Journal: :Plant physiology 2003
A Harvey Millar Joshua L Heazlewood

Plant mitochondria maintain metabolic communication with the cytosol through a family of carrier proteins. In Arabidopsis, a subset of 45 putative genes encoding members of this family have been identified based on generalized mitochondrial carrier features. No gene clusters are apparent and few of the predicted protein products have mitochondrial targeting sequences recognized by bioinformatic...

Journal: :jundishapur journal of microbiology 0
fahimeh afzal-javan department of genetics, faculty of science, university of shahrekord, shahrekord, ir iran; research institute of biotechnology, university of shahrekord, shahrekord, ir iran mohsen mobini-dehkordi department of genetics, faculty of science, university of shahrekord, shahrekord, ir iran; research institute of biotechnology, university of shahrekord, shahrekord, ir iran; department of genetics, faculty of science , university of shahrekord, shahrekord, ir iran. tel/fax. +98-3814424419

conclusions based on this similarity and our bioinformatics evaluations, this mentioned alpha-amylase gene can be expressed in s. cerevisiae as extracellular enzyme. results the presence of alpha-amylase gene in recombinant bacteria was certificated by colony-pcr method. after extraction of recombinant vector from e. coli, the competent s. cerevisiae cells were transformed using polyethylene gl...

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